A glucose electrochemical sensor based on zinc oxide (ZnO) nanorods was investigated. The hydrothermal sol–gel growth method was utilized to grow ZnO nanorods on indium tin oxide-coated glass substrates. The total active area of the working electrode was 0.3 × 0.3 cm2 where titanium metal was deposited to enhance the contact. Well aligned hexagonal structured ZnO nanorods with a diameter from 68 to 116 nm were obtained. The excitonic peak obtained from the absorbance spectroscopy was observed at ~370 nm. The dominant peak of Raman spectroscopy measurement was at 440 cm−1, matching with the lattice vibration of ZnO. The uniform distribution of the GOx and Nafion membrane that has been done using spin coating technique at 4000 rotations per minute helps in enhancing the ion exchange and increasing the sensitivity of the fabricated electrochemical sensor. The amperometric response of the fabricated electrochemical sensor was 3 s. The obtained sensitivity of the fabricated ZnO electrochemical sensor was 10.911 mA/mM·cm2 and the lower limit of detection was 0.22 µM.

The purpose of this research was to design an optical sensor for evaluating glycated hemoglobin (HbA1c) percentages in hemoglobin. The A1c sensors available in the market use invasive methods, while our device offers the possibility of non-invasive monitoring of HbA1c levels in diabetic patients. A prototype is assembled using two light emitting diodes with peak emission wavelengths of 535 nm and 593 nm, a photodiode, and a microcontroller. The proposed sensor measures the transmitted intensity in the form of an output voltage. We devise an approach to estimate the percentage of HbA1c in hemoglobin for a given solution. This estimation is based on the relative change in absorbance due to change in path length and molar absorption coefficients of hemoglobin and HbA1c, at the two wavelengths. We calculate the molar absorption coefficient of HbA1c at 535 nm and 593 nm wavelengths using the sensor, which is performed by a multiple variable regression analysis algorithm fed through the microcontroller. Specifically, the sensor output voltage with respect to the sample concentration is fitted to an exponentially decaying equation model. We used a commercial chemical assay called Control FD Glycohemoglobin A1c with known percentage HbA1c levels to verify our device measurements.

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An electrochemical glucose sensor based on zinc oxide (ZnO) nanorods is fabricated, characterized and tested. The ZnO nanorods are synthesized on indium titanium oxide (ITO) coated glass substrate, using the hydrothermal sol-gel technique. The working principle of the sensor under investigation is based on the electrochemical reaction taking place between cathode and anode, in the presence of an electrolyte. A platinum plate, used as the cathode and Nafion/Glucose Oxidase/ZnO nanorods/ITO-coated glass substrate used as anode, is immersed in pH 7.0 phosphate buffer solution electrolyte to test for the presence of glucose. Several amperometric tests are performed on the fabricated sensor to determine the response time, sensitivity and limit of detection of the sensor. A fast response time less than 3 s with a high sensitivity of 1.151 mA cm -2 mM -1 and low limit of detection of 0.089 mM is reported. The glucose sensor is characterized using the cyclic voltammetry method in the range from -0.8 -0.8 V with a voltage scan rate of 100 mV/s.

Abstract:Glucose sensor based on ITO/ZnO NRs/GOx/nafion is fabricated and tested under different glucose concentrations. Hydrothermal growth method along with sol-gel technique is used to grow high quality ZnO nanorods that have well-alignment and high density with an acceptable aspect ratio. The as-grown of ZnO nanorods are used to fabricate a working electrode that can be used for glucose detection in blood after a modification process with GOx and nafion membrane. Annealing at 110 °C helped in improves the crystallinity of the seed layer and as a result, a high density and well alignment as-grown ZnO nanorods were obtained. High sensitivity and short response time were obtained from the fabricated device with an acceptable lower limit of detection.

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